1. Introduction
In the biomedical research, the gastrointestinal tract (gut, or GI) is gaining interest for its numerous key roles, not only in nutrient and drug digestion/absorption but also in the pathways of immune response, as well as in those processes and mechanisms triggered by drug-based therapies and pharmacokinetics [
1]. Also, the GI is a protective interface in the interaction of the body with agents from the external environment, and recent advances in research are progressively describing the specific importance of gut microbiota in influencing the bidirectional communication between the central and the enteric nervous system, i.e., the gut-brain axis (GBA) [
2]. Although its increasing importance, some of small intestine’s functional mechanisms and pathologies still remain indefinite, due to the difficulties of traditional planar culture models, to take into account more than a few crucial aspects of the intestinal tracts. The failure of traditional cell-based models and in vivo tests in being predictive for the analyses of drug efficacy and toxicity, has led to the need of testing pharmaceutical compounds for a long period of time in conditions that mimic the human in vivo situation [
3] (
Figure 1).
In this respect, the development of Organ-On-Chip technologies (OOC) allows a better reproduction of a human gut, implementing microfluidic techniques which permit the handling of small amount of liquids and automated and controlled fluid flows, in order to deliver nutrients to the biological matrices. Also, for better reproducing the physiological human gut conditions, Gut-On-Chip (GOC) systems have been implemented with multiple factors/components, such as the presence of commensal microbes/pathogenic bacteria, the triggering of inflammatory responses in the presence of immune cells, or the induction of physiological movements (e.g., by applying vacuum). However, current intestine-on-a-chip systems show some disadvantages such as the inaccurate intestine’s peristalsis simulation, and the insufficient in situ sensing network to analyze procedures and effects of nutrients/stimuli on growth and adhesion of cell models in culture [
4]. Considering the idea that a multiparameter analysis could be a crucial tool for diagnostics, therapy and therapy control under the light of personalized medicine, this ambition could be addressed only integrating multiple microfluidic actuators and sensors within a single platform interacting with a an automated instrumentation [
5].
In this view, we propose a GOC platform that will be potentially integrated with a large number of analytical tools to apply and integrate many methods for detecting the fluctuation of different parameters: the membrane tightness and the passage of nutrient/drugs fluxes through it; the extracellular microenvironment parameters as the pH gradients, O2 concentration/availability, solute gradients and the plasma membrane potentials. These intertwined parameters are the basis of various physiological processes and of numerous responses to drug-based treatments. Here, to perform an in situ continuous automated sensing of microenvironment parameters, a multifunctional real-time detection device is projected. A previous evaluation has been conducted on the physiological parameters that guide cellular and gut tissue formation. Many of them still remain indefinite but are crucial for understanding the processes elicited in the response to a normal stimulus, or under an inflammatory state, or a chronic disease. The automated microfluidic control, the application and the detection of physiologically mechanical/chemical stimuli are preliminarily investigated. In addition, processes of cell adhesion, growth and polarization of a functional monolayer are described using two different human-derived epithelial cell lines.
2. Materials and Methods
In this work, the proposed Gut-on-Chip system is a modified and customized commercial Topas polymer-made platform, with two (lumen vs. blood) aligned fluidic chambers separated by a transparent and porous PET (Polyethylene terephthalate) membrane for cell culture (
Figure 2). The Membrane size is 11 × 8.5 mm
2. Membrane thickness is 23 µm, the pore dimension is about 200 nm, with a pores density of 5 × 10
8 pores/cm
2.
This microfluidic platform is equipped with transparent ITO (Indium tin Oxide) electrodes for TEER (Transepithelial Electrical Resistance) monitoring during the cell culture experiments, because TEER values are indicators of cellular barriers integrity and of tight junction dynamics in cultured cells monolayers. The measure of pH, Zn and Cu passage through the apical and basolateral chamber, will be realized by implementing miniaturized Ion Selective Electrodes (ISE). The simultaneous embedded sensors measurements and a software-controlled mechanical deflection also help in reproducing local mechanical stretches/bends/etc. To preliminarily investigate cell-to-chip interactions, we assayed cell adhesion on our PET porous membrane, and consequent proliferation, by adopting the human-derived, epithelial-like HeLa and Caco-2 cell lines. Cells were seeded on the membrane exposed to medium with no cover lid; then, the chip chamber was sealed on top and bottom sides with Corning slides equipped with electrodes, and the system was incubated for 24 h (HeLa) or 72 h (Caco-2) at 37 °C before assessing cell viability by a standard MTT assay to detect metabolic activity of cells. (
Figure 3).
3. Results
A complete, microfluidic-based and multiparameter Epithelial Gut on Chip model has been developed that could enable human intestinal epithelium growth. We basically evaluated the cell interaction, using the HeLa cell line seeded on the PET transparent porous membrane (a non-biological matrix) which expose cells to a microfluidic flow. The cell behavior on an early prototype has been observed to reduce critical aspects deriving from biological components. The sterility maintenance, the monitoring of cell viability and growth during the epithelial barriers formation and the presence of air bubbles on cell culture are challenging aspects that were evaluated using HeLa cells as preliminary study before the evaluation of a more specific cell lines such as the intestinal Caco-2 cells. Indeed, the multifunctional microsystem for monitoring epithelia parameters has been set up with proper material and microfluidics tubes and it has been primarily investigated in its ability to support cell adhesion and growth, for several days, before electrical and mechanical test on the epithelium. In our experimental setup, viable HeLa (and then Caco-2) cells have been detected by metabolization of the MTT compound producing the dark blue-to-black staining (i.e., formazan crystals in viable cells) (
Figure 3). The MTT assay is a preliminary evaluation to demonstrate a considerable efficiency of adhesion, viability and migration of human-derived intestinal cells on microfluidic devices. The optimization of in vitro conditions provides the implementation of some enabling technologies to monitor in real time important parameters that are crucial in several physiological pathways. An example is characterized by the measure of pH, or the translocation of Zn and Cu ions across the apical and basolateral chambers, that will be implemented by using miniaturized Ion Selective Electrodes (ISE). The Impedance measurements will be regularly acquired, to detect and evaluate the TEER behavior in situ. Additionally, the actuation of mechanotransduction could permit the understanding of important mechanisms of GI tissue organization; also, concomitant pharmacological assays based on nutrient/drugs intestinal interactions are under analysis. Our cell-to-device combination may represent a useful study of the epithelial tightness and the mechanotransduction in the regulatory pathways at cellular and epithelial level in the GI tissue districts, in GI drug toxicity and drug screening.